KR20230053714A - Treatment agent for elastic fibers and elastic fibers - Google Patents

Treatment agent for elastic fibers and elastic fibers Download PDF

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KR20230053714A
KR20230053714A KR1020237012146A KR20237012146A KR20230053714A KR 20230053714 A KR20230053714 A KR 20230053714A KR 1020237012146 A KR1020237012146 A KR 1020237012146A KR 20237012146 A KR20237012146 A KR 20237012146A KR 20230053714 A KR20230053714 A KR 20230053714A
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elastic fibers
agent
mass
leveling agent
mineral oil
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KR102606860B1 (en
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타케시 니시가와
케이이치로 오시마
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다케모토 유시 가부시키 가이샤
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    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
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    • D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
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    • D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
    • D06M13/03—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons with unsaturated hydrocarbons, e.g. alkenes, or alkynes
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    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
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    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
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    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
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    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/65—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing epoxy groups
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    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

본 발명이 해결하고자 하는 과제는, 탄성 섬유의 권취 시에 비산되기 어려운 탄성 섬유용 처리제 및 이러한 탄성 섬유용 처리제가 부착되어 있는 탄성 섬유를 제공한다. 본 발명의 탄성 섬유용 처리제는 광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고 테르펜 수지 및 테르펜 수지 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하는 것을 특징으로 한다. 혹은, 탄성 섬유용 처리제는 상기 적어도 하나의 평활제(A)와, 로진 및 로진 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하고, 평활제(A)가 광물유를 포함하며, 평활제(A) 중의 광물유 함유 비율이 59.5 내지 95질량%인 것을 특징으로 한다.An object to be solved by the present invention is to provide a treatment agent for elastic fibers that is difficult to scatter during winding of the elastic fibers and an elastic fiber to which such a treatment agent for elastic fibers is adhered. The treatment agent for elastic fibers of the present invention contains at least one leveling agent (A) selected from mineral oil, silicone oil and ester oil, and at least one naturally derived component (B) selected from terpene resins and terpene resin derivatives. to be characterized Alternatively, the treatment agent for elastic fibers contains the at least one leveling agent (A) and at least one naturally derived component (B) selected from rosin and rosin derivatives, the leveling agent (A) contains mineral oil, and It is characterized in that the mineral oil content rate in agent (A) is 59.5-95 mass %.

Description

탄성 섬유용 처리제 및 탄성 섬유Treatment agent for elastic fibers and elastic fibers

본 발명은 소정의 천연 유래 성분을 함유하는 탄성 섬유용 처리제 및 이러한 탄성 섬유용 처리제가 부착되어 있는 탄성 섬유에 관한 것이다.[0002] The present invention relates to a treatment agent for elastic fibers containing a predetermined naturally-derived component and an elastic fiber to which the treatment agent for elastic fibers is adhered.

예를 들어 폴리우레탄계 탄성 섬유 등의 탄성 섬유는, 다른 합성 섬유에 비해 섬유간 점착성이 강하다. 그 때문에, 예를 들어 탄성 섬유를 방사하여 패키지에 감은 후, 해당 패키지로부터 인출하여 가공 공정에 제공할 때, 패키지로부터 안정적으로 해서하기가 곤란하다는 문제가 있었다. 그 때문에, 종래보다 탄성 섬유의 평활성을 향상시키기 위하여, 탄화 수소유 등의 평활제를 함유하는 탄성 섬유용 처리제가 사용되는 경우가 있다.For example, elastic fibers such as polyurethane-based elastic fibers have stronger inter-fiber adhesiveness than other synthetic fibers. Therefore, for example, when the elastic fiber is spun and wound around a package, and then taken out from the package and subjected to a processing step, there is a problem that it is difficult to unwind stably from the package. Therefore, in order to improve the smoothness of elastic fibers more than before, the processing agent for elastic fibers containing a smoothing agent, such as hydrocarbon oil, may be used.

종래, 특허문헌 1에 개시되는 탄성 섬유용 처리제가 알려져 있다. 특허 문헌 1은, 실리콘 오일 등의 베이스 성분과, 2족 원소 금속의 2가 양이온의 산성 인산 에스테르염을 소정 비율로 함유하는 폴리우레탄 탄성 섬유용 처리제에 대하여 개시한다.Conventionally, the processing agent for elastic fibers disclosed in patent document 1 is known. Patent Document 1 discloses a treatment agent for polyurethane elastic fibers containing a base component such as silicone oil and an acidic phosphoric acid ester salt of a divalent cation of a metal of a group 2 element in a predetermined ratio.

국제 공개 제2011/105386호International Publication No. 2011/105386

그러나, 탄성 섬유용 처리제가 부여된 탄성 섬유를 와인더로 권취할 때 처리제가 비산하는 것을 억제하는 것, 즉 탄성 섬유용 처리제의 비산 억제 효과의 추가적인 향상이 요망되고 있었다.However, when winding the elastic fiber to which the processing agent for elastic fibers was provided with the winder, suppressing that a processing agent scattering, ie, the further improvement of the scattering inhibitory effect of the processing agent for elastic fibers, was desired.

본 발명자들은, 상기 과제를 해결하기 위해 연구한 결과 탄성 섬유용 처리제에 있어서, 소정의 평활제(A)와 소정의 천연 유래 성분(B)을 배합한 구성이 적합하다는 것을 발견하였다.As a result of research to solve the above problems, the inventors of the present invention have found that a composition in which a prescribed leveling agent (A) and a prescribed naturally-derived component (B) are blended is suitable for a treatment agent for elastic fibers.

상기 과제를 해결하기 위하여, 본 발명의 일 형태의 탄성 섬유용 처리제는 광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고 테르펜 수지 및 테르펜 수지 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하는 것을 특징으로 한다.In order to solve the above problems, the treatment agent for elastic fibers of one embodiment of the present invention is at least one leveling agent (A) selected from mineral oil, silicone oil and ester oil, and at least one selected from terpene resins and terpene resin derivatives. It is characterized by containing a naturally derived component (B).

상기 탄성 섬유용 처리제에 있어서, 상기 평활제(A)는 광물유를 포함하고, 상기 평활제(A) 중의 광물유 함유 비율이 55 내지 95질량%인 것이 바람직하다.In the above processing agent for elastic fibers, it is preferable that the leveling agent (A) contains mineral oil, and the mineral oil content ratio in the leveling agent (A) is 55 to 95% by mass.

상기 과제를 해결하기 위하여, 본 발명의 다른 형태의 탄성 섬유용 처리제는 광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고 로진 및 로진 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하고, 상기 평활제(A)가 광물유를 포함하고, 상기 평활제(A) 중의 광물유 함유 비율이 59.5 내지 95질량%인 것을 특징으로 한다.In order to solve the above problems, another type of treatment agent for elastic fibers of the present invention is at least one leveling agent (A) selected from mineral oil, silicone oil and ester oil, and at least one natural origin selected from rosin and rosin derivatives. It is characterized in that it contains component (B), the leveling agent (A) contains mineral oil, and the leveling agent (A) contains 59.5 to 95% by mass of mineral oil.

상기 탄성 섬유용 처리제는, 상기 평활제(A) 및 상기 천연 유래 성분(B)의 함유 비율의 합계를 100질량부라 하면, 상기 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는 것이 바람직하다.The processing agent for elastic fibers contains the naturally-derived component (B) in an amount of 0.1 to 30 parts by mass, assuming that the total content of the leveling agent (A) and the naturally-derived component (B) is 100 parts by mass. desirable.

상기 탄성 섬유용 처리제는, 탄소수 12 내지 24의 지방족 알코올과 탄소수 12 내지 24의 지방족 알코올 1몰에 대하여 탄소수 24의 알킬렌옥사이드를 1 내지 100몰의 비율로 부가시킨 고급 알코올의 알킬렌옥사이드 부가물로부터 선택되는 적어도 하나의 하이드록시 화합물(C)을 더 함유하는 것이 바람직하다.The treatment agent for elastic fibers is an alkylene oxide adduct of an aliphatic alcohol having 12 to 24 carbon atoms and a higher alcohol obtained by adding an alkylene oxide having 24 carbon atoms to 1 mole of the aliphatic alcohol having 12 to 24 carbon atoms in a ratio of 1 to 100 moles. It is preferable to further contain at least one hydroxy compound (C) selected from

상기 탄성 섬유용 처리제는, 상기 평활제(A), 상기 천연 유래 성분(B) 및 하이드록시 화합물(C)의 함유 비율의 합계를 100질량부라 하면, 상기 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는 것이 바람직하다.The processing agent for elastic fibers contains 0.1 to 30 parts of the natural component (B), when the total content of the leveling agent (A), the naturally occurring component (B), and the hydroxy compound (C) is 100 parts by mass. It is preferable to contain in the ratio of mass part.

상기 과제를 해결하기 위해, 본 발명의 다른 형태의 탄성 섬유에서는, 상기 탄성 섬유용 처리제가 부착되어 있는 것을 특징으로 한다.In order to solve the above problem, the elastic fiber of another aspect of the present invention is characterized in that the above elastic fiber processing agent is adhered.

본 발명에 따르면, 탄성 섬유용 처리제의 비산 억제 효과를 향상시킬 수 있다.ADVANTAGE OF THE INVENTION According to this invention, the scattering inhibitory effect of the processing agent for elastic fibers can be improved.

(제1 실시 형태)(First Embodiment)

이하, 본 발명의 탄성 섬유용 처리제(이하, 처리제라고도 함)를 구체화한 제1 실시 형태를 설명한다. 본 실시 형태의 처리제는, 소정의 평활제(A) 및 천연 유래 성분(B)을 함유하고, 추가로 하이드록시 화합물을 포함해도 된다.EMBODIMENT OF THE INVENTION Hereinafter, the 1st Embodiment which actualized the processing agent for elastic fibers of this invention (henceforth also referred to as a processing agent) is demonstrated. The processing agent of this embodiment contains a predetermined|prescribed leveling agent (A) and a naturally derived component (B), and may further contain a hydroxy compound.

평활제(A)는 베이스 성분으로서, 처리제에 배합되고, 탄성 섬유에 평활성을 부여하는 작용을 한다. 평활제(A)로서는 광물유, 실리콘 오일 및 에스테르 오일을 들 수 있다.The leveling agent (A), as a base component, is blended with the treatment agent and acts to impart smoothness to the elastic fibers. Mineral oil, silicone oil, and ester oil are mentioned as a leveling agent (A).

광물유로서는, 예를 들어 방향족계 탄화 수소, 파라핀계 탄화 수소, 나프텐계 탄화 수소 등을 들 수 있다. 보다 구체적으로는, 예를 들어 스핀들유, 유동 파라핀 등을 들 수 있다. 이러한 광물유는 점도 등에 따라 규정되는 시판품을 적절히 채용해도 된다.As mineral oil, an aromatic hydrocarbon, a paraffinic hydrocarbon, a naphthenic hydrocarbon, etc. are mentioned, for example. More specifically, spindle oil, liquid paraffin, etc. are mentioned, for example. As such a mineral oil, you may employ|adopt the commercial item prescribed|regulated by viscosity etc. as appropriate.

실리콘 오일의 구체예로서는, 예를 들어 디메틸실리콘, 페닐 변성 실리콘, 아미노 변성 실리콘, 아미드 변성 실리콘, 폴리에테르 변성 실리콘, 아미노폴리에테르 변성 실리콘, 알킬 변성 실리콘, 알킬아르알킬 변성 실리콘, 알킬폴리에테르 변성 실리콘, 에스테르 변성 실리콘, 에폭시 변성 실리콘, 카르비놀 변성 실리콘, 머캅토 변성 실리콘, 폴리옥시알킬렌 변성 실리콘 등을 들 수 있다. 이러한 실리콘 오일은 동점도 등에 따라 규정되는 시판품을 적절히 채용해도 된다. 동점도는 적절히 설정할 수 있지만, 25℃에서의 동점도가 2 내지 100cst(mm2/s)인 것이 바람직하다. 25℃에서의 동점도는 JIS Z 8803에 준거하여 측정된다.Specific examples of the silicone oil include, for example, dimethyl silicone, phenyl-modified silicone, amino-modified silicone, amide-modified silicone, polyether-modified silicone, aminopolyether-modified silicone, alkyl-modified silicone, alkylaralkyl-modified silicone, and alkylpolyether-modified silicone. , ester-modified silicone, epoxy-modified silicone, carbinol-modified silicone, mercapto-modified silicone, polyoxyalkylene-modified silicone, and the like. As such a silicone oil, you may employ|adopt the commercial item prescribed|regulated according to kinematic viscosity etc. as appropriate. Although the kinematic viscosity can be set appropriately, it is preferable that the kinematic viscosity at 25°C is 2 to 100 cst (mm 2 /s). The kinematic viscosity at 25°C is measured in accordance with JIS Z 8803.

에스테르 오일로서는, 특별히 제한은 없지만, 지방산과 알코올로부터 제조되는 에스테르 오일을 들 수 있다. 에스테르 오일로서는, 예를 들어 후술하는 홀수 또는 짝수의 탄화 수소기를 갖는 지방산과 알코올로부터 제조되는 에스테르 오일이 예시된다.The ester oil is not particularly limited, but ester oils produced from fatty acids and alcohols are exemplified. As an ester oil, the ester oil manufactured from the fatty acid and alcohol which have an odd-numbered or even-numbered hydrocarbon group mentioned later is illustrated, for example.

에스테르 오일의 원료인 지방산은, 그 탄소수, 분지 유무, 가수 등에 대해 특별히 제한이 없고, 예를 들어 고급 지방산이어도 되고, 시클로환을 가진 지방산이어도 되고, 방향족환을 갖는 지방산이어도 된다. 에스테르 오일의 원료인 알코올은 그 탄소수, 분지 유무, 가수 등에 대하여 특별히 제한이 없으며, 또한, 예를 들어 고급 알코올이어도, 시클로환을 갖는 알코올이어도, 방향족환을 갖는 알코올이어도 된다.The fatty acid, which is a raw material of ester oil, is not particularly limited in terms of carbon number, presence or absence of branches, valence, etc., and may be, for example, a higher fatty acid, a fatty acid having a cyclo ring, or a fatty acid having an aromatic ring. Alcohol, which is a raw material of ester oil, is not particularly limited in terms of carbon number, presence or absence of branches, valence, etc., and may be, for example, a higher alcohol, an alcohol having a cyclo ring, or an alcohol having an aromatic ring.

에스테르 오일의 구체예로서는, 예를 들어 (1) 옥틸팔미테이트, 올레일라우레이트, 올레일올레에이트, 이소트리데실스테아레이트, 이소테트라코실올레에이트 등의, 지방족 모노알코올과 지방족 모노카르복실산의 에스테르 화합물, (2) 1,6-헥산디올디데카네이트, 글리세린트리올레에이트, 트리메틸올프로판트리라우레이트, 펜타에리트리톨테트라옥타네이트 등의, 지방족 다가 알코올과 지방족 모노카르복실산의 에스테르 화합물, (3) 디올레일아젤레이트, 티오디프로피온산 디올레일, 티오디프로피온산 디이소세틸, 티오디프로피온산 디이소스테아릴 등의, 지방족 모노알코올과 지방족 다가 카르복실산의 에스테르 화합물, (4) 벤질올레에이트, 벤질라우레이트 등의, 방향족 모노알코올과 지방족 모노카르복실산의 에스테르 화합물, (5) 비스페놀 A 디라우레이트 등의, 방향족 다가 알코올과 지방족 모노카르복실산의 완전 에스테르 화합물, (6) 비스2-에틸헥실프탈레이트, 디이소스테아릴이소프탈레이트, 트리옥틸트리멜리테이트 등의, 지방족 모노알코올과 방향족 다가 카르복실산의 완전 에스테르 화합물, (7) 야자유, 채종유, 해바라기유, 대두유, 피마자유, 참깨유, 어유 및 우지 등의 천연 유지 등을 들 수 있다.Specific examples of the ester oil include, for example, (1) a mixture of aliphatic monoalcohols and aliphatic monocarboxylic acids such as octyl palmitate, oleyl laurate, oleyl oleate, isotridecyl stearate, and isotetracosyl oleate; ester compounds, (2) ester compounds of aliphatic polyhydric alcohols and aliphatic monocarboxylic acids, such as 1,6-hexanedioldidecanate, glycerin trioleate, trimethylolpropane trilaurate, and pentaerythritol tetraoctanate; (3) ester compounds of aliphatic monoalcohols and aliphatic polyhydric carboxylic acids, such as dioleyl azelate, dioleyl thiodipropionate, diisocetyl thiodipropionate, and diisostearyl thiodipropionate; (4) benzyl oleate , Ester compounds of aromatic monoalcohols and aliphatic monocarboxylic acids such as benzyllaurate, (5) complete ester compounds of aromatic polyhydric alcohols and aliphatic monocarboxylic acids such as bisphenol A dilaurate, (6) bis2 - Complete ester compounds of aliphatic monoalcohols and aromatic polyhydric carboxylic acids, such as ethylhexyl phthalate, diisostearyl isophthalate, and trioctyl trimellitate, (7) coconut oil, rapeseed oil, sunflower oil, soybean oil, castor oil, Natural fats and oils, such as sesame oil, fish oil, and beef tallow, etc. are mentioned.

이러한 평활제(A)는, 1종의 평활제를 단독으로 사용해도 되고, 2종 이상의 평활제를 조합하여 사용해도 된다.As such a leveling agent (A), one type of leveling agent may be used alone, or two or more types of leveling agents may be used in combination.

본 실시 형태에 있어서, 본 발명의 효과를 저해하지 않는 범위 내에서, 상기 이외의 평활제를 병용해도 된다. 상기 이외의 평활제로서는 공지된 것을 적절히 채용해도 된다. 상기 이외의 평활제로서는, 예를 들어 폴리올레핀 등을 들 수 있다.In this embodiment, you may use together a leveling agent other than the above within the range which does not impair the effect of this invention. As a leveling agent other than the above, you may employ a well-known thing suitably. As a leveling agent other than the above, polyolefin etc. are mentioned, for example.

폴리올레핀은, 평활 성분으로 이용되는 폴리-α-올레핀이 적용된다. 폴리올레핀의 구체예로서는, 예를 들어 1-부텐, 1-헥센, 1-데센 등을 중합하여 얻어지는 폴리-α-올레핀 등을 들 수 있다. 폴리-α-올레핀은, 시판품을 적절히 채용해도 된다.As the polyolefin, poly-α-olefin used as a smoothing component is applied. Specific examples of polyolefins include poly-α-olefins obtained by polymerizing 1-butene, 1-hexene, 1-decene and the like. As the poly-α-olefin, a commercially available product may be suitably employed.

본 실시 형태에 있어서, 평활제(A)는 광물유를 포함하는 것이 바람직하다. 평활제(A) 중에 있어서의 광물유의 함유 비율은 55 내지 95질량% 인 것이 바람직하다. 광물유 함유량을 이러한 범위로 규정함으로써 형상 특성을 보다 향상시킨다. 평활제(A) 중의 광물유 함유 비율은, 예를 들어 33.3질량% 이상, 46.2질량% 이상, 57.9질량% 이상, 59.5질량% 이상, 62.0질량% 이상, 64.7질량% 이상, 67.3질량% 이상, 67.6질량% 이상, 67.7질량% 이상, 68.4질량% 이상, 또는 69.4질량% 이상이다. 또한, 평활제(A) 중의 광물유 함유 비율은 예를 들어 88,9질량%, 69.4질량% 이하, 68.4질량% 이하, 67.7질량% 이하, 67.6질량% 이하, 67.3질량% 이하, 64.7질량% 이하, 62.0질량% 이하, 59.5질량% 이하, 57.9질량% 이하, 또는 46.2질량% 이하이다.In this embodiment, it is preferable that the leveling agent (A) contains mineral oil. It is preferable that the content rate of the mineral oil in a leveling agent (A) is 55-95 mass %. By defining the mineral oil content within this range, the shape characteristics are further improved. The mineral oil content ratio in the leveling agent (A) is, for example, 33.3% by mass or more, 46.2% by mass or more, 57.9% by mass or more, 59.5% by mass or more, 62.0% by mass or more, 64.7% by mass or more, 67.3% by mass or more, 67.6 It is mass % or more, 67.7 mass % or more, 68.4 mass % or more, or 69.4 mass % or more. In addition, the mineral oil content ratio in a leveling agent (A) is 88.9 mass % or less, 69.4 mass % or less, 68.4 mass % or less, 67.7 mass % or less, 67.6 mass % or less, 67.3 mass % or less, 64.7 mass % or less, for example. , 62.0 mass% or less, 59.5 mass% or less, 57.9 mass% or less, or 46.2 mass% or less.

천연 유래 성분(B)은 로진, 로진 유도체, 테르펜 수지 및 테르펜 수지 유도체로부터 선택되는 적어도 하나이다. 이러한 천연 유래 성분(B)은, 1종의 천연 유래 성분을 단독으로 사용해도 되고, 2종 이상의 천연 유래 성분을 조합하여 사용해도 된다. 로진은 소나무로부터 얻어지는 천연 수지이며, 아비에트산 또는 그 이성체의 혼합물을 주성분으로 한다. 로진 대신에 혹은 로진에 더하여 로진 유도체가 사용되어도 된다. 로진 유도체로서는, 아비에트산 또는 그 이성체의 수소화, 탈수소화, 아미드화, 에스테르 화합물, EO 또는 PO 부가물, 글리시딜에스테르 화합물, 아크릴화 로진, 로진 함유 디올, 부분 금속염 등을 들 수 있다. 이것들 로진 또는 로진 유도체는 연화점, 점도, 평균 분자량 등에 따라 규정되는 시판품을 적절히 채용해도 된다.The naturally-derived component (B) is at least one selected from rosin, rosin derivatives, terpene resins and terpene resin derivatives. As such a naturally-derived component (B), one type of naturally-derived component may be used alone, or two or more types of naturally-derived components may be used in combination. Rosin is a natural resin obtained from pine trees and contains abietic acid or a mixture of its isomers as a main component. Rosin derivatives may be used instead of or in addition to rosin. Examples of the rosin derivative include hydrogenation, dehydrogenation, and amidation of abietic acid or its isomer, ester compounds, EO or PO adducts, glycidyl ester compounds, acrylated rosin, rosin-containing diols, and partial metal salts. As these rosin or rosin derivatives, commercially available products prescribed according to the softening point, viscosity, average molecular weight and the like may be appropriately employed.

테르펜 수지는 소나무, 오렌지 표피로부터 채취되는 테르펜계 화합물을 원료로 하고, 양이온 중합함으로써 얻어진다. 테르펜 수지는 테르펜 모노머의 단독 중합체인 폴리테르펜 수지이어도 된다. 테르펜 수지 대신에 혹은 테르펜 수지에 더하여 테르펜 수지 유도체가 사용되어도 된다. 테르펜 수지 유도체로서는, 예를 들어 테르펜 모노머와 방향족 모노머를 공중합시킨 방향족 변성 테르펜 수지, 테르펜 모노머와 페놀류를 반응시킨 테르펜페놀 수지, 수소 첨가하여 얻어지는 수첨 테르펜 수지 등을 들 수 있다. 이것들 테르펜 수지 또는 테르펜 수지 유도체는 연화점 등에 따라 규정되는 시판품을 적절히 채용해도 된다.Terpene resin is obtained by cationic polymerization of a terpene compound obtained from the skin of a pine or orange as a raw material. The terpene resin may be a polyterpene resin that is a homopolymer of terpene monomers. A terpene resin derivative may be used instead of or in addition to the terpene resin. Examples of the terpene resin derivative include aromatic modified terpene resins obtained by copolymerizing terpene monomers and aromatic monomers, terpene phenol resins obtained by reacting terpene monomers and phenols, and hydrogenated terpene resins obtained by hydrogenation. As these terpene resins or terpene resin derivatives, commercially available products prescribed according to the softening point or the like may be appropriately used.

이것들 중에서 로진 또는 로진 유도체가 적용되는 것이 바람직하다. 로진 또는 로진 유도체가 적용됨으로써 처리제의 비산 억제 효과를 보다 향상시킬 수 있다.Among these, rosin or rosin derivatives are preferably applied. By applying rosin or a rosin derivative, the scattering inhibitory effect of the treatment agent can be further improved.

천연 유래 성분(B)의 구체예로서는, 예를 들어 중합 로진 수지(아라카와 화학 공업사 제조 "펜셀 D-160", 연화점(환구법): 160℃), 중합 로진 수지(아라카와 화학 공업사 제조) "펜셀 D-135", 연화점(환구법): 135℃), 로진 에스테르 수지(아라카와 화학 공업사 제조 "슈퍼 에스테르 A-75", 연화점(환구법): 75℃), 로진 에스테르 수지(아라카와 화학 공업사 제조 "슈퍼 에스테르 A-100", 연화점(환구법): 100℃), 로진 에스테르 수지(아라카와 화학 공업사 제조 "슈퍼 에스테르 A-125", 연화점(환구법): 125℃), 액상 로진 유도체(아라카와 화학 공업사 제조 "파인 크리스탈 ME-GH", 점도(40℃): 830mPa·s), 테르펜페놀 수지(야스하라 케미컬사 제조 "YS 폴리스터 T-130", 연화점: 130℃), 테르펜페놀 수지(야스하라 케미컬사 제조 "YS 폴리스터 T-100", 연화점: 100℃) 등을 들 수 있다.Specific examples of the naturally derived component (B) include, for example, polymerized rosin resin (manufactured by Arakawa Chemical Industries, Ltd. "Pensel D-160", softening point (ring and ball method): 160°C), polymerized rosin resin (manufactured by Arakawa Chemical Industries, Ltd.) "Pensel D -135", softening point (round and ball method): 135°C), rosin ester resin (manufactured by Arakawa Chemical Industry "Super Ester A-75", softening point (round and ball method): 75°C), rosin ester resin (manufactured by Arakawa Chemical Industry "Super Ester A-100", softening point (ring and ball method): 100 ° C.), rosin ester resin ("Super Ester A-125", softening point (ring and ball method): 125 ° C.), liquid rosin derivative (manufactured by Arakawa Chemical Industry Co., Ltd.) “Fine Crystal ME-GH”, viscosity (40° C.): 830 mPa s), terpene phenol resin (“YS Polyster T-130” manufactured by Yasuhara Chemical Co., Ltd., softening point: 130° C.), terpene phenol resin (Yasuhara Chemical "YS Polyster T-100", softening point: 100 deg.

처리제는, 평활제(A) 및 천연 유래 성분(B)의 함유 비율의 합계를 100질량부라 하면, 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는 것이 바람직하다. 이러한 범위로 규정함으로써 본 발명의 효과를 보다 향상시킬 수 있다.The processing agent preferably contains the naturally derived component (B) in an amount of 0.1 to 30 parts by mass, assuming that the total content of the leveling agent (A) and the naturally derived component (B) is 100 parts by mass. The effect of the present invention can be further improved by stipulating within such a range.

처리제는, 평활제(A) 및 천연 유래 성분(B)의 함유 비율의 합계를 100질량부라 하면, 평활제(A)를 80 내지 99.9질량부 및 천연 유래 성분(B)을 0.120질량부의 비율로 함유하는 것이 바람직하다. 이러한 범위로 규정함으로써 본 발명의 효과를 보다 향상시킬 수 있다.The processing agent is 80 to 99.9 parts by mass of the leveling agent (A) and 0.120 parts by mass of the naturally-derived component (B), assuming that the total content of the leveling agent (A) and the naturally-derived component (B) is 100 parts by mass. It is preferable to contain The effect of the present invention can be further improved by stipulating within such a range.

본 실시 형태의 처리제는, 고급 알코올로서 탄소수 12 내지 24의 지방족 알코올과 탄소수 12 내지 24의 지방족 알코올 1몰에 대하여 탄소수 2 내지 4의 알킬렌옥사이드를 1 내지 100몰의 비율로 부가시킨 고급 알코올의 알킬렌옥사이드 부가물로부터 선택되는 적어도 하나의 하이드록시 화합물(C)을 더 포함해도 된다. 이러한 하이드록시 화합물(C)을 배합함으로써 후술하는 능락(綾落) 방지성을 보다 향상시킬 수 있다.The treatment agent of the present embodiment is a higher alcohol obtained by adding a C12 to C24 aliphatic alcohol and a C2 to C4 alkylene oxide at a ratio of 1 to 100 moles per mole of the C12 to C24 aliphatic alcohol. You may further include at least one hydroxy compound (C) selected from alkylene oxide adducts. By blending such a hydroxy compound (C), it is possible to further improve the slip prevention property described later.

탄소수 12 내지 24의 지방족 알코올은, 불포화 결합 여부에 대해 특별히 제한은 없고, 직쇄상 또는 분지쇄상 탄화 수소기를 갖는 알코올이어도 되고, 시클로환을 갖는 알코올이어도 된다. 분지쇄상의 탄화 수소기를 갖는 알코올의 경우, 그 분기 위치는 특별히 제한되지 않으며, 예를 들어 α 위치가 분지된 탄소쇄이어도 되고, β 위치가 분지된 탄소쇄이어도 된다. 또한, 1급 알코올이어도, 2급 알코올이어도 된다.The aliphatic alcohol having 12 to 24 carbon atoms is not particularly limited as to whether or not it has an unsaturated bond, and may be an alcohol having a linear or branched hydrocarbon group or an alcohol having a cyclo ring. In the case of an alcohol having a branched hydrocarbon group, the branching position is not particularly limited. For example, it may be a carbon chain branched at the α position or a branched carbon chain at the β position. Further, either primary alcohol or secondary alcohol may be used.

지방족 알코올의 구체예로서는 예를 들어 라우릴알코올, 트리데실알코올, 미리스틸알코올, 펜타데실알코올, 세탄올, 스테아릴알코올, 에이코산올, 베헤닐알코올, 테트라코산올, 올레일알코올, 12-에이코실알코올, 헥사데세닐알코올, 에이코세닐알코올, 옥타데세닐알코올, 도코실알코올, 이소도데실알코올, 이소미리스틸알코올, 이소헥사데실알코올, 이소스테아릴알코올, 이소테트라코산올 등의 1가 지방족 알코올 등을 들 수 있다.Specific examples of the aliphatic alcohol include, for example, lauryl alcohol, tridecyl alcohol, myristyl alcohol, pentadecyl alcohol, cetanol, stearyl alcohol, eicosanol, behenyl alcohol, tetracosanol, oleyl alcohol, and 12-eicosyl alcohol. Monohydric aliphatic alcohols such as alcohol, hexadecenyl alcohol, eicosenyl alcohol, octadecenyl alcohol, docosyl alcohol, isododecyl alcohol, isomyristyl alcohol, isohexadecyl alcohol, isostearyl alcohol, and isotetracosanol etc. can be mentioned.

알킬렌옥사이드를 부가한 화합물이 사용되는 경우, 알킬렌옥사이드의 구체예로서는, 예를 들어 에틸렌옥사이드, 프로필렌옥사이드, 부틸렌옥사이드 등의 탄소수 2 내지 4의 알킬렌옥사이드를 들 수 있다. 고급 알코올 1몰에 대한 알킬렌옥사이드의 부가 몰수는, 바람직하게는 1 내지 100몰, 보다 바람직하게는 1 내지 50몰, 더욱 바람직하게는 1 내지 30몰이다. 또한, 알킬렌옥사이드의 부가 몰수는 투입 원료 중에 있어서의 지방족 알코올 1몰에 대한 알킬렌옥사이드의 몰수를 나타낸다.When a compound to which an alkylene oxide is added is used, specific examples of the alkylene oxide include alkylene oxides having 2 to 4 carbon atoms such as ethylene oxide, propylene oxide and butylene oxide. The number of added moles of the alkylene oxide per mole of the higher alcohol is preferably 1 to 100 moles, more preferably 1 to 50 moles, still more preferably 1 to 30 moles. In addition, the number of moles of alkylene oxide added represents the number of moles of alkylene oxide with respect to 1 mole of aliphatic alcohol in the charged raw material.

이러한 하이드록시 화합물은 한 종류의 하이드록시 화합물을 단독으로 사용해도 되고, 또는 두 종 이상의 하이드록시 화합물을 적절히 조합하여 사용해도 된다.As such a hydroxy compound, one type of hydroxy compound may be used alone, or two or more types of hydroxy compounds may be used in appropriate combination.

처리제는 평활제(A), 천연 유래 성분(B) 및 하이드록시 화합물(C)의 함유 비율의 합계를 100질량부라 하면, 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는 것이 바람직하다. 이러한 범위로 규정함으로써 본 발명의 효과를 보다 향상시킬 수 있다.If the total content of the leveling agent (A), the naturally derived component (B) and the hydroxy compound (C) is 100 parts by mass, the treatment agent preferably contains the naturally derived component (B) in an amount of 0.1 to 30 parts by mass. do. The effect of the present invention can be further improved by stipulating within such a range.

처리제는 평활제(A), 천연 유래 성분(B) 및 하이드록시 화합물(C)의 함유 비율의 합계를 100질량부라 하면, 평활제(A)를 60 내지 99.8질량부, 천연 유래 성분(B)을 0.1 내지 20질량부 및 하이드록시 화합물(C)을 0.1 내지 20질량부의 비율로 함유하는 것이 바람직하다. 이러한 범위로 규정함으로써 본 발명의 효과를 보다 향상시킬 수 있다.The processing agent is 60 to 99.8 parts by mass of the leveling agent (A), if the total content of the leveling agent (A), the naturally derived component (B) and the hydroxy compound (C) is 100 parts by mass, the naturally occurring component (B) 0.1 to 20 parts by mass and the hydroxy compound (C) in an amount of 0.1 to 20 parts by mass. The effect of the present invention can be further improved by stipulating within such a range.

(제2 실시 형태)(Second Embodiment)

다음으로, 본 발명에 따른 탄성 섬유를 구체화한 제2 실시 형태에 대해 설명한다. 본 실시 형태의 탄성 섬유에는 제1 실시 형태의 처리제가 부착되어 있다. 탄성 섬유에 대한 제1 실시 형태의 처리제(용매 불포함)의 부착량은 특별히 제한은 없지만, 본 발명의 효과를 보다 향상시킨다는 점에서 0.1 내지 10질량%의 비율로 부착되어 있는 것이 바람직하다.Next, a second embodiment embodying the elastic fiber according to the present invention will be described. The processing agent of the first embodiment is adhered to the elastic fiber of the present embodiment. The amount of adhesion of the treatment agent (without solvent) of the first embodiment to the elastic fibers is not particularly limited, but is preferably 0.1 to 10% by mass from the viewpoint of further improving the effect of the present invention.

탄성 섬유로서는, 특별히 제한은 없지만, 예를 들어 폴리에스테르계 탄성 섬유, 폴리아미드계 탄성 섬유, 폴리올레핀계 탄성 섬유, 폴리우레탄계 탄성 섬유 등을 들 수 있다. 이것들 중에서도 폴리우레탄계 탄성 섬유가 바람직하다. 이러한 경우에, 본 발명의 효과의 발현을 보다 높게 할 수 있다.The elastic fibers are not particularly limited, and examples thereof include polyester-based elastic fibers, polyamide-based elastic fibers, polyolefin-based elastic fibers, and polyurethane-based elastic fibers. Among these, polyurethane-based elastic fibers are preferable. In such a case, the expression of the effect of the present invention can be made higher.

본 실시 형태의 탄성 섬유 제조 방법은, 제1 실시 형태의 처리제를 탄성 섬유에 급유하는 것을 포함한다. 처리제의 급유 방법으로서는, 희석하지 않고 니트 급유법에 의해, 탄성 섬유의 방사 공정에 있어서 탄성 섬유에 부착시키는 방법이 바람직하다. 부착 방법으로서는, 예를 들어 롤러 급유법, 가이드 급유법, 스프레이 급유법 등의 공지된 방법을 적용할 수 있다. 급유 롤러는 통상, 구금으로부터 권취 트래버스까지의 사이에 위치하는 것이 일반적이며, 본 실시 형태의 제조 방법에도 적용될 수 있다. 이것들 중에서도 연신 롤러와 연신 롤러 사이에 위치하는 급유 롤러로 제1 실시 형태의 처리제를 탄성 섬유, 예를 들어 폴리우레탄계 탄성 섬유에 부착시키는 것이 효과의 발현이 현저하기 때문에 바람직하다.The elastic fiber manufacturing method of the present embodiment includes lubricating the elastic fiber with the treatment agent of the first embodiment. As a method for supplying the treatment agent with oil, a method for adhering the treatment agent to the elastic fiber in the spinning step of the elastic fiber by a nit supplying method without dilution is preferable. As an attachment method, well-known methods, such as a roller lubrication method, a guide lubrication method, and a spray lubrication method, can be applied, for example. The oil supply roller is generally located between the spinneret and the take-up traverse, and can also be applied to the manufacturing method of the present embodiment. Among these, it is preferable to make the treatment agent of the first embodiment adhere to elastic fibers, for example, polyurethane-based elastic fibers, by means of a stretching roller and an oil supply roller positioned between the stretching rollers, since the expression of the effect is remarkable.

본 실시 형태에 적용되는 탄성 섬유 자체의 제조 방법은, 특별히 한정되지 않고, 공지된 방법으로 제조가 가능하다. 예를 들어 습식 방사법, 용융 방사법, 건식 방사법 등을 들 수 있다. 이것들 중에서도, 탄성 섬유의 품질 및 제조 효율이 우수하다는 관점에서 건식 방사법이 바람직하게 적용된다.The manufacturing method of the elastic fiber itself applied to this embodiment is not specifically limited, It can manufacture by a well-known method. For example, wet spinning method, melt spinning method, dry spinning method, etc. are mentioned. Among these, the dry spinning method is preferably applied from the viewpoint of excellent quality and production efficiency of elastic fibers.

본 실시 형태의 처리제 및 탄성 섬유의 작용 및 효과에 대해 설명한다.Actions and effects of the treatment agent and elastic fibers of the present embodiment will be described.

(1) 본 실시 형태의 처리제는 광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고 로진, 로진 유도체, 테르펜 수지 및 테르펜 수지 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유한다. 따라서, 처리제가 부여된 탄성 섬유를 특히 와인더로 권취할 때의 처리제의 비산 억제 효과를 향상시킬 수 있다. 또한, 처리제가 부여된 탄성 섬유의 형상 특성, 특히 치즈 형상으로 권취 시의 형상 특성을 향상시킬 수 있다. 또한, 처리제가 부여된 탄성 섬유의 능락 방지성을 향상시킬 수도 있다.(1) The treatment agent of the present embodiment includes at least one leveling agent (A) selected from mineral oil, silicone oil and ester oil, and at least one naturally derived component selected from rosin, rosin derivatives, terpene resins and terpene resin derivatives ( B) contains Therefore, the scattering suppression effect of the processing agent at the time of winding the elastic fiber to which the processing agent was provided especially with a winder can be improved. In addition, the shape characteristics of the elastic fibers to which the treatment agent is applied can be improved, especially the shape characteristics at the time of winding into a cheese shape. In addition, it is also possible to improve the anti-drip property of the elastic fibers to which the treatment agent is applied.

또한, 상기 실시 형태는 이하와 같이 변경해도 된다. 상기 실시 형태 및 이하의 변경예는 기술적으로 모순되지 않는 범위에서 서로 조합하여 실시할 수 있다.In addition, you may change the said embodiment as follows. The above embodiments and the following modifications can be implemented in combination with each other within a range that is not technically contradictory.

·상기 실시 형태의 처리제에는 본 발명의 효과를 저해하지 않는 범위 내에 있어서 처리제의 품질 유지를 위한 안정화제, 제전제, 연결제, 산화 방지제, 자외선 흡수제 등의 통상적으로 처리제에 이용되는 성분을 더 배합해도 된다.The processing agent of the above embodiment further contains components commonly used in processing agents such as a stabilizer for maintaining the quality of the processing agent, an antistatic agent, a linking agent, an antioxidant, and an ultraviolet absorber within a range that does not impair the effect of the present invention. You can do it.

실시예Example

이하, 본 발명의 구성 및 효과를 보다 구체적으로 설명하기 위하여 실시예 등을 들지만, 본 발명이 이러한 실시예로 한정된다는 것은 아니다. 또한 이하의 실시예 및 비교예의 설명에 있어서 부는 질량부를, %는 질량%를 의미한다.Hereinafter, Examples and the like are given to explain the configuration and effects of the present invention in more detail, but the present invention is not limited to these Examples. In addition, in the description of the following Examples and Comparative Examples, part means part by mass and % means mass %.

시험 구분 1 (탄성 섬유용 처리제의 조제)Test Division 1 (preparation of treatment agent for elastic fibers)

각 실시예, 각 비교예에 이용한 처리제는, 표 1에 나타내는 각 성분을 사용하고, 하기 조제 방법에 의해 조제하였다.The processing agent used for each Example and each comparative example was prepared by the following preparation method using each component shown in Table 1.

광물유(40℃에 있어서의 레드우드 점도계에서의 점도가 60초) (A-1) 55부(%) 및 디메틸실리콘(10cst(mm2/s), 25℃) (A-3) 30부(%)와 천연 유래 성분으로서 중합 로진 수지(B-1) 7부(%), 하이드록시 화합물로서 이소스테아릴알코올(C-1) 8부(%)를 잘 혼합하여 균일하게 함으로써 실시예 1의 처리제를 조제하였다.Mineral oil (viscosity of 60 seconds in a redwood viscometer at 40 ° C.) (A-1) 55 parts (%) and dimethyl silicone (10 cst (mm 2 /s), 25 ° C.) (A-3) 30 parts ( %), 7 parts (%) of polymerized rosin resin (B-1) as a natural component, and 8 parts (%) of isostearyl alcohol (C-1) as a hydroxy compound. A treatment agent was prepared.

실시예 2 내지 15, 17, 19 내지 22, 참고예 16, 18, 비교예 1, 2는 실시예 1과 마찬가지로 하여 평활제, 천연 유래 성분 및 하이드록시 화합물을 표 1에 나타낸 비율로 혼합함으로써 처리제를 조제하였다.Examples 2 to 15, 17, 19 to 22, Reference Examples 16 and 18, and Comparative Examples 1 and 2 were carried out in the same manner as in Example 1 by mixing a leveling agent, a naturally-derived component and a hydroxy compound in the ratio shown in Table 1, thereby treating the treatment agent. was prepared.

각 예의 처리제 중에 있어서의 평활제(A), 천연 유래 성분(B) 및 하이드록시 화합물(C)의 각 성분의 종류, 각 성분의 함유 비율의 합계를 100%라 했을 경우에 있어서의 각 성분의 비율을 표 1의 "평활제(A)"란, "천연 유래 성분(B)"란, "하이드록시 화합물(C)"란에 각각 나타낸다.Type of each component of the leveling agent (A), naturally occurring component (B) and hydroxy compound (C) in the treatment agent of each case, and each component in the case where the sum of the content ratio of each component is 100% The proportions are shown in the columns of "leveler (A)", "naturally derived component (B)" and "hydroxy compound (C)" in Table 1, respectively.

Figure pct00001
Figure pct00001

표 1에 기재하는 A-1 내지 A-4, B-1 내지 B-8, C-1, C-2의 상세는 이하와 같다.Details of A-1 to A-4, B-1 to B-8, C-1 and C-2 described in Table 1 are as follows.

(평활제(A))(Leveler (A))

A-1: 광물유(40℃에 있어서의 레드우드 점도계에서의 점도가 60초)A-1: Mineral oil (viscosity in redwood viscometer at 40 ° C. is 60 seconds)

A-2: 광물유(40℃에 있어서의 레드우드 점도계에서의 점도가 100초)A-2: Mineral oil (viscosity in redwood viscometer at 40 ° C. is 100 seconds)

A-3: 디메틸실리콘(10cst(mm2/s), 25℃)A-3: Dimethylsilicon (10cst (mm 2 /s), 25°C)

A-4: 이소트리데실스테아레이트A-4: isotridecylstearate

(천연 유래 성분(B))(naturally derived ingredient (B))

B-1: 중합 로진 수지(아라카와 화학 공업사 제조 "펜셀 D-160", 연화점: 160℃)B-1: polymerized rosin resin (“Pencell D-160” manufactured by Arakawa Chemical Industry, softening point: 160° C.)

B-2: 중합 로진 수지(아라카와 화학 공업사 제조 "펜셀 D-135", 연화점: 135℃)B-2: polymerized rosin resin (“Pencell D-135” manufactured by Arakawa Chemical Industries, Ltd., softening point: 135° C.)

B-3: 로진 에스테르 수지(아라카와 화학 공업사 제조 "슈퍼 에스테르 A-75", 연화점: 75℃)B-3: rosin ester resin (“Super Ester A-75” manufactured by Arakawa Chemical Industry, softening point: 75° C.)

B-4: 로진 에스테르 수지(아라카와 화학 공업사 제조 "슈퍼 에스테르 A-100", 연화점: 100℃)B-4: rosin ester resin (“Super Ester A-100” manufactured by Arakawa Chemical Industry, softening point: 100° C.)

B-5: 로진 에스테르 수지(아라카와 화학 공업사 제조 "슈퍼 에스테르 A-125", 연화점: 125℃)B-5: Rosin ester resin (“Super Ester A-125” manufactured by Arakawa Chemical Industry, softening point: 125° C.)

B-6: 액상 로진 유도체(아라카와 화학 공업사 제조 "파인 크리스탈 МE-GH", 점도(40℃) : 830mPa·s)B-6: Liquid rosin derivative (“Pine Crystal МE-GH” manufactured by Arakawa Chemical Industry, Viscosity (40° C.): 830 mPa s)

B-7: 테르펜페놀 수지(야스하라 케미칼사 제조 "YS폴리스터 T-130", 연화점: 130℃)B-7: terpene phenol resin (“YS Polyster T-130” manufactured by Yasuhara Chemical Co., Ltd., softening point: 130° C.)

B-8: 테르펜페놀 수지(야스하라 케미칼사 제조 "YS폴리스터 T-100", 연화점: 100℃)B-8: terpene phenol resin (“YS Polyster T-100” manufactured by Yasuhara Chemical, softening point: 100° C.)

(하이드록시 화합물(C))(hydroxy compound (C))

C-1: 이소스테아릴알코올C-1: isostearyl alcohol

C-2: 이소트리데실알코올의 에틸렌옥사이드 3몰 부가물C-2: ethylene oxide 3 mole adduct of isotridecyl alcohol

시험 구분 2(탄성 섬유의 제조)Test division 2 (manufacture of elastic fibers)

분자량 1000의 폴리테트라메틸렌글리콜과 디페닐메탄디이소시아네이트로부터 얻은 프리폴리머를 디메틸포름아미드 용액 중에서 에틸렌디아민에 의해 쇄 신장 반응시켜 농도 30%의 방사 도프를 얻었다. 이 방사 도프를 방사 구금으로부터 가열 가스류 중에 있어서 건식 방사하였다. 건식 방사한 폴리우레탄계 탄성 섬유에 시험 구분 1에서 조제한 처리제를 롤러 오일링법으로 니트 급유하였다. 이어서 처리제를 부여한 폴리우레탄계 탄성 섬유를 패키지에 권취하여 20데니어(모노필라멘트)의 처리가 완료된 폴리우레탄계 탄성 섬유를 얻었다. 처리제 부착량의 조절은 급유 롤러의 회전수를 조정함으로써 모두 5%가 되도록 하였다.A prepolymer obtained from polytetramethylene glycol and diphenylmethane diisocyanate having a molecular weight of 1000 was chain-extended with ethylenediamine in a dimethylformamide solution to obtain a spinning dope having a concentration of 30%. This spinning dope was dry-spun from a spinneret in a heated gas stream. The dry-spun polyurethane-based elastic fiber was nit-lubricated with the treatment agent prepared in test section 1 by the roller oiling method. Subsequently, the polyurethane-based elastic fiber to which the treatment agent was applied was wound around a package to obtain a 20-denier (monofilament) treated polyurethane-based elastic fiber. The amount of treatment agent applied was adjusted to 5% by adjusting the number of revolutions of the oil supply roller.

이렇게 하여 얻어진 탄성 섬유, 롤러 급유한 건식 방사 폴리우레탄계 탄성 섬유 패키지를 이용하여 비산 억제 효과, 탄성 섬유의 형상 특성, 능락 방지성을 이하에 설명하는 바와 같이 하여 평가하였다.Using the elastic fibers obtained in this way and the roller-lubricated dry-spun polyurethane-based elastic fiber package, the scattering suppression effect, the shape characteristics of the elastic fibers, and the slip prevention properties were evaluated as described below.

시험 구분 3(탄성 섬유의 평가)Test division 3 (elastic fiber evaluation)

·비산 억제 효과Scattering suppression effect

얻어진 방사 직후의 건식 방사 폴리우레탄계 탄성 섬유 패키지(500g 롤)를 송출 속도 100m/분, 권취 속도 250m/분으로 30분 감았을 경우의 와인더 부근에서 인정되는 처리제의 비산량을 육안으로 관찰하였다. 비산량의 관찰은, 와인더 아래에 두꺼운 종이를 깔고, 두꺼운 종이에 부착된 처리제를 관찰함으로써 행하였다. 이하의 기준으로 평가한 결과를 표 1의 "비산"란에 나타낸다.The amount of scattering of the treatment agent found near the winder when the obtained dry-spun polyurethane-based elastic fiber package (500 g roll) immediately after spinning was wound for 30 minutes at a feed speed of 100 m/min and a take-up speed of 250 m/min was visually observed. The amount of scattering was observed by placing thick paper under the winder and observing the processing agent adhering to the thick paper. The results evaluated according to the criteria below are shown in the "Dispersion" column of Table 1.

◎(양호): 비산이 인정되지 않는 경우◎ (Good): When scattering is not recognized

○(가능): 약간의 비산이 인정된 경우○ (possible): When some scattering is recognized

×(불량): 상당한 비산이 인정된 경우× (defective): When significant scattering is recognized

·형상 특성의 평가･Evaluation of shape characteristics

20데니어(모노필라멘트)의 폴리우레탄계 탄성 섬유에 시험 구분 1에서 조제한 처리제를 롤러 급유법으로 5.0% 부착시켰다. 그리고 권취 속도 550m/분으로 길이 57mm의 원통형 지관에, 권취 폭 42mm를 부여하는 트래버스 가이드를 통해 서페이스 드라이브 권취기를 이용하여 500g 권취하여, 폴리우레탄계 탄성 섬유 패키지를 얻었다.5.0% of the treatment agent prepared in test section 1 was adhered to 20 denier (monofilament) polyurethane-based elastic fibers by a roller lubrication method. Then, 500 g was wound around a cylindrical paper tube having a length of 57 mm at a winding speed of 550 m/min using a surface drive winder through a traverse guide giving a winding width of 42 mm, thereby obtaining a polyurethane-based elastic fiber package.

얻어진 폴리우레탄계 탄성 섬유 패키지(500g 롤)에 대해서 권취 폭의 최대값(Wmax)과 최소폭(Wmin)을 계측하고, 양쪽의 차이(Wmax-Wmin)로부터 벌지를 구하여 하기의 기준으로 평가하였다. 그 결과를 표 1의 '형상'란에 나타낸다.The maximum value (Wmax) and the minimum width (Wmin) of the winding width of the obtained polyurethane-based elastic fiber package (500 g roll) were measured, and the bulge was obtained from the difference (Wmax-Wmin) of both, and evaluated according to the following criteria. The results are shown in the 'Shape' column of Table 1.

◎(양호): 벌지가 3mm 미만인 경우◎ (Good): When the bulge is less than 3 mm

○(가능): 벌지가 3mm 이상 6mm 미만인 경우○ (possible): If the bulge is 3 mm or more and less than 6 mm

×(불가): 벌지가 6mm 이상인 경우× (no): When the bulge is 6 mm or more

·능락 방지성의 평가･Evaluation of fall prevention

얻어진 방사 직후의 건식 방사 폴리우레탄계 탄성 섬유 패키지(500g 롤)를 송출 속도 20m/분, 권취 속도 40m/분으로 1000m롤 감았을 경우의 패키지의 능락에 따른 단사 횟수를 다음 기준으로 평가하였다. 그 결과를 표 1의 "능락 방지성"란에 나타낸다.When the obtained dry-spun polyurethane-based elastic fiber package (500 g roll) immediately after spinning was wound with a 1000 m roll at a feed speed of 20 m/min and a take-up speed of 40 m/min, the number of single yarns according to the tangle of the package was evaluated according to the following criteria. The results are shown in the column of "drip prevention" in Table 1.

◎(양호): 능락에 의한 단사가 0회인 경우◎ (Good): In the case of single yarn by neungrak 0 times

○(가능): 능락에 의한 단사가 1회 이상 3회 미만인 경우○ (possible): In the case of single yarn by neungrak 1 or more times and less than 3 times

×(불량): 능락에 의한 단사가 3회 이상인 경우× (defective): In the case of three or more single yarns due to neungrak

표 1의 각 비교예에 대한 각 실시예의 평가 결과에서도 명확한 바와 같이, 본 발명의 처리제에 의하면, 처리제가 부여된 탄성 섬유로부터의 처리제의 비산을 억제할 수 있다. 또한 형상 특성 및 능락 방지성을 향상시킬 수 있다.As is also clear from the evaluation results of each example for each comparative example in Table 1, according to the processing agent of the present invention, scattering of the processing agent from the elastic fibers to which the processing agent is applied can be suppressed. In addition, it is possible to improve shape characteristics and slip prevention.

본 발명은 이하의 양태도 포함한다.The present invention also includes the following aspects.

(부기 1)(Note 1)

광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고, 로진, 로진 유도체, 테르펜 수지, 및 테르펜 수지 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하는 것을 특징으로 하는 탄성 섬유용 처리제.Characterized in that it contains (A) at least one leveling agent selected from mineral oil, silicone oil and ester oil, and (B) at least one naturally derived component selected from rosin, rosin derivatives, terpene resins, and terpene resin derivatives. A treatment agent for elastic fibers.

(부기 2)(Note 2)

상기 천연 유래 성분(B)이 로진 및 로진 유도체로부터 선택되는 적어도 하나인, 부기 1에 기재된 탄성 섬유용 처리제.The treatment agent for elastic fibers according to Appendix 1, wherein the naturally-derived component (B) is at least one selected from rosin and rosin derivatives.

(부기 3)(Note 3)

상기 평활제(A)가 광물유를 포함하고, 상기 평활제(A) 중의 광물유 함유 비율이 55 내지 95질량%인, 부기 1 또는 2에 기재된 탄성 섬유용 처리제.The processing agent for elastic fibers as described in supplementary note 1 or 2 whose said leveling agent (A) contains mineral oil, and the mineral oil content rate in the said leveling agent (A) is 55-95 mass %.

(부기 4)(Bookkeeping 4)

상기 평활제(A) 및 상기 천연 유래 성분(B)의 함유 비율의 합계를 100질량부라 하면, 상기 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는 부기 1 내지 3 중 어느 하나에 기재된 탄성 섬유용 처리제.Assuming that the total content of the leveling agent (A) and the naturally derived component (B) is 100 parts by mass, in any one of Appendix 1 to 3 containing the naturally derived component (B) in an amount of 0.1 to 30 parts by mass. The treatment agent for elastic fibers described.

(부기 5)(Bookkeeping 5)

추가로, 탄소수 12 내지 24의 지방족 알코올과, 탄소수 12 내지 24의 지방족 알코올 1몰에 대해 탄소수 2 내지 4의 알킬렌옥사이드를 1 내지 100몰의 비율로 부가시킨 고급 알코올의 알킬렌옥사이드 부가물로부터 선택되는 적어도 하나의 하이드록시 화합물(C)을 함유하는 부기 1 내지 3 중 어느 하나에 기재된 탄성 섬유용 처리제.Further, from an alkylene oxide adduct of an aliphatic alcohol having 12 to 24 carbon atoms and a higher alcohol obtained by adding an alkylene oxide having 2 to 4 carbon atoms in a ratio of 1 to 100 mol with respect to 1 mol of the aliphatic alcohol having 12 to 24 carbon atoms. The treatment agent for elastic fibers according to any one of Appendix 1 to 3 containing at least one selected hydroxy compound (C).

(부기 6)(Note 6)

상기 평활제(A), 상기 천연 유래 성분(B) 및 하이드록시 화합물(C)의 함유 비율의 합계를 100질량부라 하면, 상기 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는 부기 5에 기재된 탄성 섬유용 처리제.If the total content of the leveling agent (A), the naturally occurring component (B) and the hydroxy compound (C) is 100 parts by mass, the naturally occurring component (B) is contained in an amount of 0.1 to 30 parts by mass. The processing agent for elastic fibers of 5.

(부기 7)(Bookkeeping 7)

부기 1 내지 6 중 어느 하나에 기재된 탄성 섬유용 처리제가 부착되어 있는 것을 특징으로 하는 탄성 섬유.An elastic fiber characterized by adhering the treatment agent for elastic fibers according to any one of Supplementary Notes 1 to 6.

Claims (7)

광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고 테르펜 수지 및 테르펜 수지 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하는 것을 특징으로 하는 탄성 섬유용 처리제.A treatment agent for elastic fibers characterized by containing (A) at least one leveling agent selected from mineral oil, silicone oil and ester oil, and (B) at least one naturally derived component selected from terpene resins and terpene resin derivatives. 제1항에 있어서, 상기 평활제(A)가 광물유를 포함하고, 상기 평활제(A) 중의 광물유 함유 비율이 55 내지 95질량%인, 탄성 섬유용 처리제.The processing agent for elastic fibers of Claim 1 whose said leveling agent (A) contains mineral oil, and the mineral oil content rate in the said leveling agent (A) is 55-95 mass %. 광물유, 실리콘 오일 및 에스테르 오일로부터 선택되는 적어도 하나의 평활제(A), 그리고 로진 및 로진 유도체로부터 선택되는 적어도 하나의 천연 유래 성분(B)을 함유하고, 상기 평활제(A)가 광물유를 포함하고, 상기 평활제(A) 중의 광물유 함유 비율이 59.5 내지 95질량%인 것을 특징으로 하는 탄성 섬유용 처리제.At least one leveling agent selected from mineral oil, silicone oil and ester oil (A), and at least one naturally derived component selected from rosin and rosin derivatives (B), wherein the leveling agent (A) comprises mineral oil And, the mineral oil content ratio in the said leveling agent (A) is 59.5-95 mass %, The processing agent for elastic fibers characterized by the above-mentioned. 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 평활제(A) 및 상기 천연 유래 성분(B)의 함유 비율의 합계를 100질량부라 하면, 상기 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는, 탄성 섬유용 처리제.The natural component (B) according to any one of claims 1 to 3, when the total content of the leveling agent (A) and the naturally occurring component (B) is 100 parts by mass, the amount of the naturally occurring component (B) is 0.1 to 30 The processing agent for elastic fibers contained in the ratio of parts by mass. 제1항 내지 제3항 중 어느 한 항에 있어서, 추가로 탄소수 12 내지 24의 지방족 알코올, 및 탄소수 12 내지 24의 지방족 알코올 1몰에 대해, 탄소수 2 내지 4의 알킬렌옥사이드를 1 내지 100몰의 비율로 부가시킨 고급 알코올의 알킬렌옥사이드 부가물로부터 선택되는 적어도 하나의 하이드록시 화합물(C)을 함유하는, 탄성 섬유용 처리제.The method according to any one of claims 1 to 3, further comprising 1 to 100 moles of an alkylene oxide having 2 to 4 carbon atoms per 1 mole of the aliphatic alcohol having 12 to 24 carbon atoms and the aliphatic alcohol having 12 to 24 carbon atoms. A treatment agent for elastic fibers containing at least one hydroxy compound (C) selected from alkylene oxide adducts of higher alcohols added at a ratio of: 제5항에 있어서, 상기 평활제(A), 천연 유래 성분(B) 및 하이드록시 화합물(C)의 함유 비율의 합계를 100질량부라 하면, 상기 천연 유래 성분(B)을 0.1 내지 30질량부의 비율로 함유하는, 탄성 섬유용 처리제.The method according to claim 5, when the total content of the leveling agent (A), the naturally occurring component (B) and the hydroxy compound (C) is 100 parts by mass, the naturally occurring component (B) is 0.1 to 30 parts by mass The processing agent for elastic fibers contained in the ratio. 제1항 내지 제6항 중 어느 한 항에 기재된 탄성 섬유용 처리제가 부착되어 있는 것을 특징으로 하는 탄성 섬유.An elastic fiber characterized by adhering the treatment agent for elastic fibers according to any one of claims 1 to 6.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003013362A (en) * 2001-04-26 2003-01-15 Du Pont Toray Co Ltd Polyurethane-based elastic fiber and method for producing the same
JP2006037303A (en) * 2004-07-29 2006-02-09 Sanyo Chem Ind Ltd Oil formulation for treating fiber
KR20080061130A (en) * 2006-12-28 2008-07-02 주식회사 효성 A spinning oil used in manufacturing spandex including rosin compound
WO2011105386A1 (en) 2010-02-25 2011-09-01 松本油脂製薬株式会社 Agent for treating polyurethane elastic fiber, and polyurethane elastic fiber

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2591570A (en) * 1949-04-08 1952-04-01 Socony Vacuum Oil Co Inc Cutting oil
US3697440A (en) * 1969-06-27 1972-10-10 Diamond Shamrock Corp Defoamer compositions containing organic particles
GB8923285D0 (en) * 1989-10-16 1989-12-06 Unilever Plc Fabric conditioning article
FR2794476B1 (en) * 1999-06-07 2001-11-16 Rhodia Chimie Sa USE OF TERPENIC POLYALCOXYL DERIVATIVES IN THE TREATMENT OF TEXTILE FIBERS
JP2002003527A (en) * 2000-06-16 2002-01-09 Yasuhara Chemical Co Ltd Modified terpene resin, and resin composition containing the same
JP2002046021A (en) * 2000-08-02 2002-02-12 Nippon Mitsubishi Oil Corp Electric discharge machining fluid
JP5936293B1 (en) * 2015-05-12 2016-06-22 竹本油脂株式会社 Dry-spun polyurethane elastic fiber
CN106008765A (en) * 2016-06-27 2016-10-12 梧州市嘉盈树胶有限公司 Method for producing terpene resin with high softening point

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003013362A (en) * 2001-04-26 2003-01-15 Du Pont Toray Co Ltd Polyurethane-based elastic fiber and method for producing the same
JP2006037303A (en) * 2004-07-29 2006-02-09 Sanyo Chem Ind Ltd Oil formulation for treating fiber
KR20080061130A (en) * 2006-12-28 2008-07-02 주식회사 효성 A spinning oil used in manufacturing spandex including rosin compound
WO2011105386A1 (en) 2010-02-25 2011-09-01 松本油脂製薬株式会社 Agent for treating polyurethane elastic fiber, and polyurethane elastic fiber

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